Reaction equation
[CH2:1]([NH2:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].N1[CH:14]=[CH:13]C=CC=1.C(Cl)(=[O:17])C>C(Cl)Cl>[CH2:3]([CH2:2][C:1]([NH2:8])=[O:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:13][CH3:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of n-heptylamine (10.31 g, 89.4 mmol) in 100 mL CH2Cl2 was cooled in an ice bath. Pyridine (7.5 mL, 92.7 mmol) was added. Acetyl chloride (8.0 mL, 11 mmol) was gradually added over the course of 2 min. The ice bath was removed and the solution was allowed to warm to room temperature. After 1 h, water (100 mL) was added, and the organic layer was separated. The aqueous layer was extracted with 100 mL CH2Cl2. The combined organic extracts were washed with 10% aqueous HCl solution, saturated NaHCO3 solution and then saturated NaCl solution. The solution was dried over MgSO4 and evaporated to give n-heptyl acetamide as a colorless liquid (13.73 g, 98% yield.
Workup
- customThe ice bath was removed
- additionwater (100 mL) was added
- customthe organic layer was separated
- extractionThe aqueous layer was extracted with 100 mL CH2Cl2
- washThe combined organic extracts were washed with 10% aqueous HCl solution, saturated NaHCO3 solution
- dry with materialThe solution was dried over MgSO4
- customevaporated
Sources & evidence
- ORD record
- ord-3ea181f910d240c480c75b3da9364082
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220884B2
Linked notes
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